CN1291785A - Manufacturing method of semiconductor device - Google Patents

Manufacturing method of semiconductor device Download PDF

Info

Publication number
CN1291785A
CN1291785A CN00100943A CN00100943A CN1291785A CN 1291785 A CN1291785 A CN 1291785A CN 00100943 A CN00100943 A CN 00100943A CN 00100943 A CN00100943 A CN 00100943A CN 1291785 A CN1291785 A CN 1291785A
Authority
CN
China
Prior art keywords
semiconductor film
catalyst material
crystallization
nickel
film
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
CN00100943A
Other languages
Chinese (zh)
Other versions
CN1150595C (en
Inventor
张宏勇
鱼地秀贵
高山彻
山崎舜平
竹村保彦
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Semiconductor Energy Laboratory Co Ltd
Original Assignee
Semiconductor Energy Laboratory Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Semiconductor Energy Laboratory Co Ltd filed Critical Semiconductor Energy Laboratory Co Ltd
Publication of CN1291785A publication Critical patent/CN1291785A/en
Application granted granted Critical
Publication of CN1150595C publication Critical patent/CN1150595C/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/02Manufacture or treatment of semiconductor devices or of parts thereof
    • H01L21/02104Forming layers
    • H01L21/02365Forming inorganic semiconducting materials on a substrate
    • H01L21/02656Special treatments
    • H01L21/02664Aftertreatments
    • H01L21/02667Crystallisation or recrystallisation of non-monocrystalline semiconductor materials, e.g. regrowth
    • H01L21/02675Crystallisation or recrystallisation of non-monocrystalline semiconductor materials, e.g. regrowth using laser beams
    • H01L21/02686Pulsed laser beam
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/02Manufacture or treatment of semiconductor devices or of parts thereof
    • H01L21/02104Forming layers
    • H01L21/02365Forming inorganic semiconducting materials on a substrate
    • H01L21/02367Substrates
    • H01L21/0237Materials
    • H01L21/02422Non-crystalline insulating materials, e.g. glass, polymers
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/02Manufacture or treatment of semiconductor devices or of parts thereof
    • H01L21/02104Forming layers
    • H01L21/02365Forming inorganic semiconducting materials on a substrate
    • H01L21/02436Intermediate layers between substrates and deposited layers
    • H01L21/02439Materials
    • H01L21/02488Insulating materials
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/02Manufacture or treatment of semiconductor devices or of parts thereof
    • H01L21/02104Forming layers
    • H01L21/02365Forming inorganic semiconducting materials on a substrate
    • H01L21/02436Intermediate layers between substrates and deposited layers
    • H01L21/02439Materials
    • H01L21/02491Conductive materials
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/02Manufacture or treatment of semiconductor devices or of parts thereof
    • H01L21/02104Forming layers
    • H01L21/02365Forming inorganic semiconducting materials on a substrate
    • H01L21/02436Intermediate layers between substrates and deposited layers
    • H01L21/02494Structure
    • H01L21/02496Layer structure
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/02Manufacture or treatment of semiconductor devices or of parts thereof
    • H01L21/02104Forming layers
    • H01L21/02365Forming inorganic semiconducting materials on a substrate
    • H01L21/02436Intermediate layers between substrates and deposited layers
    • H01L21/02494Structure
    • H01L21/02496Layer structure
    • H01L21/02502Layer structure consisting of two layers
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/02Manufacture or treatment of semiconductor devices or of parts thereof
    • H01L21/02104Forming layers
    • H01L21/02365Forming inorganic semiconducting materials on a substrate
    • H01L21/02518Deposited layers
    • H01L21/02521Materials
    • H01L21/02524Group 14 semiconducting materials
    • H01L21/02532Silicon, silicon germanium, germanium
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/02Manufacture or treatment of semiconductor devices or of parts thereof
    • H01L21/02104Forming layers
    • H01L21/02365Forming inorganic semiconducting materials on a substrate
    • H01L21/02656Special treatments
    • H01L21/02664Aftertreatments
    • H01L21/02667Crystallisation or recrystallisation of non-monocrystalline semiconductor materials, e.g. regrowth
    • H01L21/02672Crystallisation or recrystallisation of non-monocrystalline semiconductor materials, e.g. regrowth using crystallisation enhancing elements
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L27/00Devices consisting of a plurality of semiconductor or other solid-state components formed in or on a common substrate
    • H01L27/02Devices consisting of a plurality of semiconductor or other solid-state components formed in or on a common substrate including semiconductor components specially adapted for rectifying, oscillating, amplifying or switching and having potential barriers; including integrated passive circuit elements having potential barriers
    • H01L27/12Devices consisting of a plurality of semiconductor or other solid-state components formed in or on a common substrate including semiconductor components specially adapted for rectifying, oscillating, amplifying or switching and having potential barriers; including integrated passive circuit elements having potential barriers the substrate being other than a semiconductor body, e.g. an insulating body
    • H01L27/1214Devices consisting of a plurality of semiconductor or other solid-state components formed in or on a common substrate including semiconductor components specially adapted for rectifying, oscillating, amplifying or switching and having potential barriers; including integrated passive circuit elements having potential barriers the substrate being other than a semiconductor body, e.g. an insulating body comprising a plurality of TFTs formed on a non-semiconducting substrate, e.g. driving circuits for AMLCDs
    • H01L27/1259Multistep manufacturing methods
    • H01L27/127Multistep manufacturing methods with a particular formation, treatment or patterning of the active layer specially adapted to the circuit arrangement
    • H01L27/1274Multistep manufacturing methods with a particular formation, treatment or patterning of the active layer specially adapted to the circuit arrangement using crystallisation of amorphous semiconductor or recrystallisation of crystalline semiconductor
    • H01L27/1281Multistep manufacturing methods with a particular formation, treatment or patterning of the active layer specially adapted to the circuit arrangement using crystallisation of amorphous semiconductor or recrystallisation of crystalline semiconductor by using structural features to control crystal growth, e.g. placement of grain filters
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L29/00Semiconductor devices specially adapted for rectifying, amplifying, oscillating or switching and having potential barriers; Capacitors or resistors having potential barriers, e.g. a PN-junction depletion layer or carrier concentration layer; Details of semiconductor bodies or of electrodes thereof ; Multistep manufacturing processes therefor
    • H01L29/66Types of semiconductor device ; Multistep manufacturing processes therefor
    • H01L29/66007Multistep manufacturing processes
    • H01L29/66075Multistep manufacturing processes of devices having semiconductor bodies comprising group 14 or group 13/15 materials
    • H01L29/66227Multistep manufacturing processes of devices having semiconductor bodies comprising group 14 or group 13/15 materials the devices being controllable only by the electric current supplied or the electric potential applied, to an electrode which does not carry the current to be rectified, amplified or switched, e.g. three-terminal devices
    • H01L29/66409Unipolar field-effect transistors
    • H01L29/66477Unipolar field-effect transistors with an insulated gate, i.e. MISFET
    • H01L29/66742Thin film unipolar transistors
    • H01L29/6675Amorphous silicon or polysilicon transistors
    • H01L29/66757Lateral single gate single channel transistors with non-inverted structure, i.e. the channel layer is formed before the gate

Landscapes

  • Engineering & Computer Science (AREA)
  • Physics & Mathematics (AREA)
  • Power Engineering (AREA)
  • Microelectronics & Electronic Packaging (AREA)
  • Manufacturing & Machinery (AREA)
  • Condensed Matter Physics & Semiconductors (AREA)
  • General Physics & Mathematics (AREA)
  • Computer Hardware Design (AREA)
  • Chemical & Material Sciences (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Optics & Photonics (AREA)
  • Ceramic Engineering (AREA)
  • Materials Engineering (AREA)
  • Recrystallisation Techniques (AREA)
  • Thin Film Transistor (AREA)

Abstract

The present invention relates to a method for fabricating a semiconductor device comprising the steps of carrying out the selectivity partial contact between a catalyzing substance and a semiconductor film containing amorphous silicon, wherein the catalysis is able to promote the crystallization of the semiconductor film; annealing the semiconductor film with catalyzing substance so that the semiconductor film is crystallized; and corrupting the catalyzing substance from the top surface of the semiconductor film, wherein the semiconductor film is basically not effected by the corrosion step.

Description

The manufacture method of semiconductor device
The application divides an application.The original bill applying date is to be on February 15th, 1994, and application number is 94103243.40.Denomination of invention is " semiconductor and a manufacture method thereof ".
The present invention relates to thin-film device, such as film-insulated gate field-effect transistor (hereinafter to be referred as be " thin-film transistor " or " TFT ") etc. semiconductor device, and manufacture method.
Being used for such as the film of the crystal silicon semiconductor of thin-film devices such as TFT is with manufactured down known to before this: used its temperature of kind equipment of electric furnace to keep being not less than 600 ℃, through 12 hours or longer, make by plasma CVD (chemical vapor deposition) or hot CVD and form the amorphous silicon membrane crystallization.Film with the crystalline solid Si semiconductor of enough high-quality (for example: excellent field-effect mobility and high reliability) only makes noncrystal membrane stand could obtain after the heat treatment of longer time.
Yet these wait to solve for the method for the prior art that obtains the crystal silicon semiconductor film has many problems.One of problem is a poor efficiency, and production cost is increased.For example, the step of crystallization needs 24 hours, and the processing time of establishing a substrate was preferably in 2 minutes, 720 substrates of so once essential processing.Yet once manageable maximum substrate number is limited to 50 in common tube furnace; Then substrate will be with finishing processing in 30 minutes as can be known only to use an equipment (reaction tube) when actual treatment.In other words, if want every substrate in 2 minutes, to finish reaction, then at least 15 reaction tubes must be arranged.This shows that this method has improved investment cost, has therefore increased production cost, because the investment depreciation cost is too big.
Heat treatment temperature is another problem that will consider.In general, quartz glass substrate or the alkali-free borate glass substrate that comprises pure silica used in the manufacturing of a TFT, as the #7059 glass substrate made by Corning Incorporated company (hereinafter to be referred as be " Corning#7059 substrate ").Preceding a kind of substrate has the heat resistance such as excellence, can handle with the habitual wafer technique the same manner that is used in semiconductor integrated circuit.Yet it is very expensive, and its price forms increase exponentially with the chip area increase.So the application of quartz glass substrate now is limited to the quite little TFT integrated circuit of area.
On the other hand, no alkali borosilicate glass substrate is inexpensive compared with those substrates by the quartz glass manufacturing, and still, they are having shortcoming aspect its heat resistance.Because the alkali-free glass substrate is out of shape under the temperature of from 550 to 650 ℃ of scopes, particularly, because the material bought easily reaches 600 ℃ even lower temperature and just is out of shape low, anyly will on substrate, cause irreversible contraction and curl in the heat treatment below 600 ℃.These distortion appear at its catercorner length especially significantly and surpass on 10 cun the substrate.Therefore, believe the heat treatment that under temperature is 550 ℃ or lower situation, to finish the Si semiconductor film, and the time is in 4 hours, to reduce total production cost.
In view of situation recited above, an object of the present invention is to provide a kind of semiconductor, wherein Shang Mian problem overcomes, and the method for making it is provided.Another object of the present invention provides a kind of method of using this kind semiconductor to make semiconductor device.
The invention provides a kind of method, it is characterized in that it comprises: on the amorphous silicon film or one have on it irregular crystalline state can be considered to amorphous (for example, a kind of state that comprises that crystalline portion and amorphous fraction mix) form on the film skim, particle, bunch, line, and analog, they contain in nickel, iron, cobalt, platinum and the palladium at least a; The structure of this formation is lower than the crystallization temperature of common amorphous silicon in temperature, preferably low 20 to 150 ℃, perhaps under temperature is not higher than usually vitrification point as the glass material of substrate, for example, anneals at 580 ℃ or following.
Each schematic diagram of the structure in the step successively that Fig. 1 (A) illustrates obtaining by one embodiment of the present of invention (example 1) method of seeing from above to 1 (C).
Each section structure (step of selected crystallization) schematic diagram in the step successively that Fig. 2 (A-1), 2 (A-2), 2 (B), 2 (C) and 2 (D) illustrate that the other method by another embodiment of the present invention obtains;
Fig. 3 has represented the crystalline rate of silicon and the relation between the crystallization temperature;
Fig. 4 represents the result by the Raman scattering wave spectrum of the crystal silicon film of an example acquisition;
Fig. 5 represents the X-ray diffraction figure by the crystal silicon film of an example acquisition;
Fig. 6 (A-1), 6 (A-2), 6 (B), 6 (C) and 6 (D) illustrate by another embodiment of the present invention and make each the section structural representation in the step successively that obtains in the semiconductor approach;
Fig. 7 (A) illustrates by another embodiment of the present invention to 7 (D) and makes each structural representation of section in the step successively that obtains in the semiconductor approach; And
Fig. 8 represents the CONCENTRATION DISTRIBUTION of nickel in the crystal silicon film.
Usually the method that is used for the silicon fiml crystallization of suggestion comprises from the solid phase epitaxial of seed crystal living Long, using crystalline solid island film is nuclear, as at JP-A-1-214110 (term " JP-A " Be used for herein the expression " unexamined disclosed Japanese patent application ") in disclosed. So And finding does not have in fact the crystal growth to take place under 600 ℃ or lower temperature. Silica-based General its crystallization is performed such in the situation of material: be in amorphous strand one Dawn is cut off, and the again combination between the molecule that does not cut off in the state of setting up thereafter, These molecules are combined into the part of crystal by molecules. Will be once the strand that cuts off It is sizable maintaining necessary energy, therefore, keeps the molecule of cut-out separated from each other This step be potential barrier in the reaction of crystallization. This energy equivalence is in about 1000 ℃ of temperature Lower heating time a few minutes of degree, perhaps under about 600 ℃ of temperature, heated tens hours. Owing to add Hot time exponentially doubly depends on heating-up temperature, finds in fact not to be higher than 600 in temperature ℃, for example realize in the time of 500 ℃ that particularly crystallization is impracticable. Solid phase epitaxial crystallization The prior art concept this solution of problem way can not be provided.
The inventor etc. bypass the solid-phase crystallization theory of usually having set up and have investigated and use catalytic reaction Reduce the method for the barrier energy of preceding method. The inventor etc. notice nickel (Ni), iron (Fe), cobalt (Co), platinum (Pt) and palladium (Pd) have affinity well with silicon, so they can be easy Ground forms silicide. To the situation of nickel, form easily nickle silicide (NiSix with silicon; Wherein 0.4 ≤ X≤2.5). And the lattice paprmeter that the inventor etc. notice nickle silicide is close to silicon Lattice paprmeter. Therefore, the free energy of ternary crystalline solid silicon-nickel silicide non-crystalline silicon system Be used to prove the non-crystalline silicon react in mutually border with nickle silicide easily and according to the following formula Chemical reaction forms nickle silicide and silicon metal: Non-crystalline silicon (silicon A)+nickle silicide (silicon B)---→
Nickle silicide (silicon A)+silicon metal (silicon B) wherein, silicon A and silicon B represent the position of silicon atom.The potential barrier of this reaction is sufficiently low, and reaction occurs under the low temperature.
The response prompting that top reaction equation is represented nickle atom amorphous silicon is become silicon metal.In fact, be reflected at temperature and be not higher than under 580 ℃ and begin, even can see that reaction betides low temperature to 450 ℃.More typically, crystallization can be implemented under the temperature that is lower than 20 to 150 ℃ of common recrystallized amorphous silicon temperature, certainly, accelerates with crystallization temperature rising crystallization.This can be clear that (will use in this figure example below) on Fig. 3.Similarly the result is using platinum (Pt), and iron (Fe) also can obtain in the situation of cobalt (Co) or palladium (Pd).
By method of the present invention, the growth that it is characterized in that crystal is isotropically to carry out in circular scope.This is because nickle atom and analog thereof isotropically move, and is therefore different with this crystallization of growing along the lattice plane of crystal of common crystal.
In pressing method of the present invention, nickel, iron, cobalt, platinum or palladium, with granulosa, particle, bunch etc. form or simple metal or silicide, be rendered as island, band shape, wire or point-like form, it can become the starting point that expansion and extension crystallization district go to its peripheral part.
As mentioned above, the silicon metal that obtains in last method is different with the usual way that is obtained by solid-phase epitaxial growth, and it also has excellent structural continuity and is similar to the crystal of monocrystalline silicon.So the silicon metal that is obtained by this law is applicable to that manufacturing is as the TFT semiconductor device.Moreover, found when the material that contains nickel, iron, cobalt, platinum or palladium is evenly distributed on the substrate, to be difficult to be improved the film of degree of crystallinity, because countless crystallization illustration is arranged.The material of having used nickeliferous, iron, cobalt, platinum or palladium in the homogeneous film of topped all surfaces situation and used the difference between the situation of the material that is island, band shape, line or point-like style can clearly observe by means of Raman scattering wave spectrum and X-ray diffraction analysis.Confirmed that with these analytical methods good silicon metal can obtain by method of the present invention.
Being used as raw-material amorphous silicon film in method for crystallising of the present invention, preferably to contain hydrogen concentration low as far as possible.Yet,, between the hydrogen concentration of the hydrogen concentration of original amorphous silicon film and the silicon fiml obtained by crystallization, can't see connection relation clearly because hydrogen discharges with crystallization gradually from amorphous silicon film.Hydrogen concentration by the crystal silicon film that obtains by the inventive method typically is in 1 * 10 15Individual atom cm -3To atomicity 5% between.Still there is the silicon fiml of excellent crystallinity to obtain each concentration to 1 * 10 with the concentration that reduces carbon, oxygen, nitrogen 19Cm -3Or it is lower.So the material of nickeliferous, iron, cobalt or platinum must consider that this point selects.
Top catalytic elements, that is, itself does not help silicon nickel, iron, cobalt, platinum and palladium.Therefore, their concentration preferably is suppressed to minimum as far as possible.Observe with SIMS (secondary ion mass spectroscopy view), the inventor etc. find that by further investigation to being used for the concentration as semi-conductive these elements of semiconductor device such as TFT, characteristic that collateral security is good and viewpoint of reliability preferably are controlled at 1 * 10 15Atom cm -3In 1% atoms range, preferably 1 * 10 15To 1 * 10 19Atom cm -3In the scope.If the concentration of catalytic metal element drops on this below scope, will there be enough crystallizations to occur.On the other hand, concentration goes beyond the scope, and just will obtain all poor semiconductor of characteristic and reliability.
Because nickle silicide is at the end of crystallization, as result, in hydrofluoric acid or hydrochloric acid, dissolve easily by the reaction of top formulate, nickel can use these acid to handle and reduce from substrate.
The film of the material of nickeliferous, iron, cobalt, platinum or palladium can constitute with method any physics or chemistry.For example, the method for using vacuum equipment as gas deposition, sputter, and CVD (chemical vapor deposition) be available, the method for perhaps in atmosphere, finishing, as spin coating, dipping (lining), the operation skill in using a kitchen knife in cookery, silk screen printing, to reach spray pyrolysis etc. also be available.
Particularly, spin coating or infusion process can provide the film with uniform thickness, and in addition, the concentration of the film of gained can accurately be controlled.The solution that is used to above method comprises those acetates with nickel, iron, cobalt, platinum or palladium, nitrate or carboxylate dissolving or is distributed to such as the solvent of water, alcohol (lower alcohol or higher alcohol) and can makes in petroleum solvent saturated hydrocarbons or unsaturated hydrocarbons.
But, used such material after, the oxygen and the carbon that probably are contained in the salt may diffuse into silicon fiml, they may damage the characteristic of semiconductor of silicon fiml.Therefore, after studying, use TGAs such as the inventor and difference thermal analysis system (differential thermal analysis) learn, by suitably selecting material, such substance is decomposed under 450 ℃ or following temperature and is produced oxide or element, and do not have this material further to spread, this diffusion may make them move into silicon fiml.Particularly, when decomposing in such as reducing atmospheres such as nitrogen, this class salt of acetate and nitrate is found and produces metal element under 400 ℃ or following temperature.Find these salts at first by in oxygen atmosphere, decompose producing oxide, but at last oxygen taken off when inhaling that these salt produce metal element under high temperature.
Used the crystal silicon film of making by the inventive method in this based semiconductor device of picture TFT, can see that the end of crystalline portion is unfavorable for making semiconductor device.As described above, this is because run into together mutually at the end of crystalline portion from the crystallization front portion that a plurality of starting points begin, thereby occurs the big grain boundary or the crystallization of discontinuity aspect crystallinity.In addition, the nickel concentration of this part is high.So the figure of semiconductor device and the figure of nickeliferous coating are optimized in advance in the method requirement of making semiconductor device by the present invention, promptly give the starting point of optimizing crystallization earlier.
The present invention consults following nonrestrictive example and describes in detail.Should be understood that the present invention can not be interpreted as being limited.Example 1
This example relates to a kind of method, is used to form a plurality of island nickel films on the Corning#7059 glass substrate, is that starting point makes the amorphous silicon film crystallization with these films then.This example also provides a kind of method, is used to use the crystal silicon film by obtaining above to make TFT.Island nickel film can be with any one forms in two kinds of methods; Be about to island nickel film and be formed on the amorphous silicon film, or under the amorphous silicon film.Fig. 2 (A-1) expression provides the method for island nickel film under amorphous silicon film.Fig. 2 (A-2) expression is formed at method on the amorphous silicon film with them.The corrosion that but should be taken into account the nickel film that is forming on the amorphous silicon in one method of back is carried out as a step after formation MULTI-LAYER NICKEL film.What come on is although that with very little amount, undesirable nickle silicide forms by the reaction between nickel and the amorphous silicon.Because if nickle silicide is retained on the silicon fiml, the silicon fiml that enough high-crystallinities are arranged that satisfies the object of the invention just can not obtain, and residual nickle silicide must be removed it fully with hydrochloric acid, hydrofluoric acid and similar thing.Thereby obtain compared with the thinner amorphous silicon film of the film that originally was deposited as.
In any case nickel or nickle silicide can be with any make figure in two kinds of common known methods, promptly, a kind of is etch, after being included in formation nickel film, make the photoetching glue pattern with the photoetching method, the nickel membrane portions that will do not covered by photoresist erodes again; Another kind is to peel off method, be included in the nickel film formed thereon before, make the photoresist figure with the photoetching method, remove following photoresist again so that form the nickel film selectively.
Preceding a kind of method about Fig. 2 (A-1) does not have the problems referred to above.Process according to said method, the nickel film except the island part also preferably eliminates fully.And then substrate is handled with oxidation regional except island areas and is suppressed the influence of remaining nickel with oxygen plasma or ozone and analog thereof.
In any case, two kinds of methods all comprise with plasma CVD deposit the thick silica basement membrane 1B of 2000 on Corning#7059 substrate 1A, and amorphous silicon film 1 is further deposited thereon, and thickness is 200 to 3000 , and preferably thickness is between 500 to 1500 .Amorphous film can come to remove dehydrogenation by this film is annealed in 0.1 to 2 hour under 350 to 450 ℃ temperature from amorphous film makes its easier crystallization.
In process about Fig. 2 (A-1), form before the amorphous silicon film 1, one deck nickel film is deposited to thickness 50 to 1000 with sputtering method, is preferably 100 to 500 .Resulting nickel film is scribed into island nickel district 2.The final structure of seeing from above is shown in Fig. 1 (A).
Each all is made into 2 μ m island nickel part 2Square size and to get each other distance be 5 to 50 μ m particularly, for example, is 20 μ m.Replace nickel also can obtain similar effects with nickle silicide.Also having, is 100 to 500 ℃ with substrate in temperature range, and preferably scope is that 180 to 250 ℃ of following heating can pay off.This is summed up as the tightness degree that increases combination between silicon oxide film bottom and the nickel film, also is summed up as by the reaction between silica and the nickel to form nickle silicide.Replace silica can obtain similar result with silicon nitride, carborundum or silicon.
Resulting structure temperature range in nitrogen atmosphere is 450 to 650 ℃, particularly, for example, is 550 ℃ of annealing 8 hours.Intermediateness during heating is shown in Fig. 2 (B).Be advanced to middle body from the visible nickel of Fig. 2 (B) from the island nickel film that is positioned at Fig. 2 (A) end and form nickle silicide 3A.And, also can see nickel the part 3 of process silicon metal is provided.So crystallization is finished on such point, meets mutually at this point from the forefront of two different island parts, and stays residual nickle silicide 3A in the center, this is shown in Fig. 2 (C).
Fig. 4 and Fig. 5 have respectively provided the Raman scattering wave spectrogram and the X-ray diffractogram of last crystal silicon film.In Fig. 4, be marked with the Raman wave spectrum of the curve of C-Si mark, i.e. the wave spectrum of monocrystalline silicon corresponding to standard specimen.Curve (a) and (b) show the Raman wave spectrum of the silicon fiml that obtains by the inventive method respectively and the Raman wave spectrum of noncrystalline domain.The result can know the silicon crystal that can provide by method of the present invention is provided thus.
Fig. 1 (B) is given to resulting structure vertical view till this step.Nickle silicide 3A is corresponding to grain boundary 4 in Fig. 2 (C).Continue annealing again, nickel moves and concentrates at island zone line 5 partly along grain boundary 4, and this island nickel part is all formed by its original shape distortion.
Silicon metal can be obtained by each step described above.Yet this is inadvisable, because silicon metal has the nickel that diffuses into the semiconductor coating from the nickle silicide 3A that forms thus.So, preferably use this class of hydrofluoric acid or hydrochloric acid, the corrosive agent corrosion is not because these acid influence silicon fiml.Be shown in Fig. 2 (D) by the resulting structure in corrosion back.On the position of original grain boundary, a groove 4A has been arranged.Forming semiconductor regions (active layer and similar layer) by this way, to have groove to be present between each semiconductor regions be worthless.An example of TFT configuration is shown in Fig. 1 (C).On the other hand, grid wiring 7 can stride across grain boundary.
Amorphous silicon film by above method with 2 * 2 μ m 2The nickel district carries out crystallization as the zone of departure.Studied the relation of crystalline rate and annealing temperature.Crystalline rate is calculated like this: mensuration is used for the crystallization forward position and reaches the necessary annealing time of nickelic district 10 to 50 μ m distance.Its result provides as an example in Fig. 3.For the two kinds of amorphous silicon films that have that compare its result, a kind of thickness is 500 , and another kind of thickness is 1500 .Certainly, crystalline rate is also higher when annealing temperature is higher.Crystalline rate is also relevant with thickness, increases the easier generation of thickness crystallization.Because actual semiconductor typically is of a size of 50 μ m or following, if crystalline rate essential 20 μ m/ hours was at least finished in annealing in 5 hours.Thickness there is the silicon of 1500 , reads to such an extent that annealing temperature at least should be at 550 ℃ or higher from Fig. 3.Example 2
This example relates to the method for having used the formation that is described in the example 1 to make crystal silicon film, and just the degree of crystallinity of film is further made film crystallization at the beginning improved by irradiation with laser beam by heating.Except the laser irradiation step, that describes in other steps and condition and the example 1 is the same.Used also corresponding the same in symbol among Fig. 6 and numeral and the example 1.
Consult Fig. 6, make each step of method for semiconductor by this example and be described below.Step (A-1) to (B) is the same with explanation in example 1.After having carried out the step of Fig. 6 (B), crystal can be in cross growth, laser beam irradiation it so that further improve the degree of crystallinity of silicon fiml.Like this, a kind of KrF excites the laser of unit to be operated laser beam irradiation with wavelength 248nm and pulsewidth 20nsec in the crystal silicon film of making before this, with its crystallization of further acceleration.Illuminating laser beam output energy density is 200 to 400mJ/cm 2, be exemplified as 250mJ/cm in this situation 2During laser beam irradiation, the substrate heating remains on 150 to 400 ℃, shines 2 times more specifically as under 200 ℃ of temperature, to strengthen the effect of laser beam irradiation.
Available laser comprises that those excite the laser that is operated in wavelength 308nm of first laser generation and the laser that is operated in wavelength 193nm that excites first laser to take place from ArF from XeCl except above-mentioned KrF excites first laser.In addition, the also alternative laser of high light carries out irradiation.Particularly, use RTA (rapid thermal annealing) and comprise that infrared irridiation also is effectively, because it can heat silicon fiml selectively at short notice.
Thus, there is the silicon fiml of good degree of crystallinity to obtain with above said any method.The crystal region 3 that the previous result as heating anneal obtains finds to become the degree of crystallinity that can further improve silicon fiml.On the other hand, when heating anneal, there is not the regional (not shown) of crystallization to find because the result of laser radiation produces polycrystalline film.The Raman scattering wave spectrogram represents silicon fiml change, but the degree of crystallinity of the polycrystalline film that obtains thus is very poor.And then, showed that with transmission electron microscope observation a large amount of microlites that form do not make its crystallization because of heat treatment in being subjected to the film of laser radiation.In contrast, relatively big oriented crystallization crystal grain is found the film 3 through thermal annealing and laser irradiation that has constituted by the present invention's acquisition.
After having finished laser radiation, to the front end 3A of crystal growth with hydrofluoric acid or hcl corrosion.Structure by the corrosion gained is shown in Fig. 6 (D).
Thereby TFT is made by the silicon fiml that is processed into the island form.On this TFT, observe the device property of obvious raising.Particularly, to obtain field-effect mobility be 50 to 90cm to the N-channel TFT that adopts the crystallisation step described in example 1 to obtain 2/ vs, and threshold voltage is 3 to 8V.These numerical value and be 150 to 200cm by the resulting mobility of N-channel TFT that this example is made 2/ vs and threshold voltage are 0.5 to 1.5V to be tangible contrast.Mobility improves considerably, and the fluctuation of threshold voltage is also significantly reduced.
In the past, foregoing high-caliber TFT characteristic like this must obtain from amorphous silicon film by laser crystallization.But the silicon fiml that is obtained by the prior art laser crystallization makes characteristics fluctuation.And then crystallization process requires the laser energy density 350mJ/cm of irradiation 2Or higher, temperature is at 400 ℃ or higher, so it is not suitable for batch process.Opposite with usual method, by this example make TFT method can the two all be lower than the numerical value of corresponding usual method in substrate temperature and energy density.Therefore, the inventive method is applicable to batch process.And then, also the same even by the device quality that this method obtains with the device quality that the common solid state growth crystallisation of using heating anneal obtains.So, can stably obtain the TFT of homogeneous quality.
In the present invention, find that crystallization takes place insufficiently when nickel concentration is low.Yet, use laser radiation can compensate inadequate crystallization according to this routine method.So, even when nickel concentration is low, also can obtain high-quality TFT satisfactorily.The device that this demonstration contains low concentration nickel can be realized, can obtain the device of excellent electrical stability and reliability.Example 3
This example relates to a kind of method, uses the upper surface of the solution lining amorphous silicon film that contains catalytic elements that catalytic elements is imported amorphous film, and this catalytic elements has been quickened the crystallization of amorphous silicon film.In this example.Nickel is used as catalytic elements.This example except the method that imports nickel and description in example 1 just the same beyond.Crystallisation step and each step subsequently are the same with description in example 1.Corresponding to the structure of above substrate, seeing of Fig. 1 also with example 1 the same.
Fig. 7 illustrates the manufacture process by sequential steps of the present invention.One deck silicon oxide film 1B is deposited on 10 * 10cm as the substrate coating 2On the square Corning#7059 glass substrate 1A, and then make 1000 thickness amorphous silicon films 1 thereon by the plasma CVD method deposition.
Silicon oxide film 13 is deposited over and reaches 1200 thickness on the prepared amorphous silicon film, so that one deck mask to be provided.Silicon oxide film 13 is thinned to that 500 thickness can be employed and without any problem, by adopting fine and close rete, can does film thinner.
The common photoetching of prepared silicon oxide film 13 usefulness is made the method for figure and is made figure on demand.Then, thin silicon oxide film 12 forms with ultraviolet (UV) line irradiation deposition in oxygen atmosphere.Particularly, silicon oxide film 13 usefulness ultraviolet irradiations were made in 5 minutes.Silicon oxide film 12 believes that its thickness is 20 to 50 .
Form above-mentioned silicon oxide film, improve the wettability of figure with the solution of following coated.Therefore, the acetate that contains 100ppm weight nickel molten 11 with a 5ml drops in 10 * 10cm 2On the surface of substrate.Spinner 10 forms moisture rete uniformly on all surfaces that makes substrate 10 seconds that turns round under the 50rpm speed.Spinner 10 reruns in addition under 2000rpm speed after substrate keeps 5 minutes again and carried out centrifuge dripping in 60 seconds.Substrate can bear speed on spinner be 0 to the rotation of 150rpm.This step is shown in Fig. 7 (A).
After removing silicon oxide masking film 13, made structure is subjected to 550 ℃ of temperature under nitrogen atmosphere heat treatment made amorphous silicon film 1 crystallization in 4 hours.By this way, crystallization can be gone along laterally expanding to the zone that nickel is not imported into from the zone 14 that nickel is imported into.
Consult Fig. 7 (B), visible crystallization is from zone 14 beginnings of direct importing nickel, and as seen it laterally carries out towards middle body.Crystal silicon film 3 obtains in this way.Form silicon nitride at regional 3A, the growth front of crystal meets mutually there.
After this, the regional 3A of nickel oxide removes with hydrofluoric acid or hydrochloric acid.The structure that is obtained by corrosion is shown in Fig. 7 (D).
The distribution of the concentration of nickel is shown in Fig. 8 in this zone.Nickel concentration in the crystal silicon film of having finished crystallization is measured with SIMS (ion microprobe), and the nickel concentration that has confirmed the zone 14 that nickel directly imports has than in the taller order of magnitude of concentration shown in Figure 8 or above value.
Can also or be equivalent to its high light with illuminating laser beam,, further improve the degree of crystallinity of the crystal silicon film that obtains above as mode same in the front example 2.In the situation of example 2, the form of film is damaged by laser radiation, because the crystal grain of nickle silicide, approximately from 0.1 to 10 μ m is precipitated out from the nickel film that quite high nickel concentration is arranged.Yet because the nickel concentration of nickel film can be than resulting much lower in example 1 and 2, the precipitation of nickle silicide and consequent rough surface can be avoided taking place.
The nickel concentration that is shown in Fig. 8 can be controlled with the nickel concentration that changes institute's coated solution.In the present invention, the nickel concentration in the solution is not controlled.In the present invention, the nickel concentration in the solution is adjusted to 100ppm.But confirmed even dropped to the 10ppm crystallization and also take place when concentration.With the solution of the nickel that contains 10ppm concentration, crystallization takes place in the same way.In this situation, the nickel concentration that is shown in Fig. 8 can further reduce a number grade., using to contain the low excessively solution of nickel concentration and shortened along the distance of the direction crystal growth of laterally pointing out by arrow, is undesirable therefore.
Acetate solution is used as the solution that contains catalytic elements in this example.But other available solution comprise and are selected from various aqueous solutions, and the solution that contains organic solvent.Catalytic elements must be comprised that it can be dispersed in the solution simply as a compound.
The solvent that is used for catalytic elements can be selected from polar solvent, that is, and and water, alcohol, acid, and ammoniacal liquor.
When nickel was used as catalytic elements, nickel was sneaked in the polar solvent with the compound form of nickel.The compound of nickel is selected from respectively: nickelous bromide, nickel acetate, ethanedioic acid nickel, nickelous carbonate, nickel chloride, nickel iodide, nickel nitrate, nickelous sulfate, nickel formate, acetylacetonate nickel, 4-ring ethyl butyric acid nickel, nickel oxide, and nickel hydroxide.
Solvent can be selected from following non-polar solven: benzene, toluene, dimethylbenzene, carbon tetrachloride, chloroform, and ether.
In this case, nickel is contained in the solution with the compound form of nickel, and this compound is selected from acetylacetonate nickel, and 2-ethyl hexane nickel.
Also can in containing the solution of catalytic elements, add surfactant.Surfactant solution can increase the degree of adhesion of solution to the silicon oxide film surface, and the control adsorptivity.Surfactant can give and being added on earlier on the surface that will be covered.If elemental nickel is used as catalytic elements, then must give being dissolved in earlier in the acid to obtain its solution.
Replace containing the solution that is dissolved in the nickel in the solution fully, available a kind of emulsion, that is, a kind of material that comprises decentralized medium, the compound of wherein even dispersed metal nickel by powder or nickel also can be used.
Also can be with material beyond the nickel as catalytic elements.
The solution that contains non-polar solven, that is, the toluene solution of 2-ethyl hexane nickel can directly be used on the surface of amorphous silicon film.In the case, can be commonly used to constitute protective layer with a kind of material as bonding agent.But excessive application of adhesive is disturbed catalytic elements to shift on the contrary and is entered in the amorphous silicon.
It is relevant with solution type that catalytic elements is mixed the amount of solution, and having approx with nickel is 1 to 200ppm by weight, best for by weight from 1 to 50ppm.The decision of the scope of this additive will be considered the situation of the nickel concentration and the hydrofluoric acid resistant of crystalline film.
As previously mentioned, the present invention can make amorphous silicon in addition lower temperature crystallization within a short period of time aspect found new era.And the inventive method is applicable to batch process, also has, and it can be realized with prevailing instrument, equipment and method.Therefore it is to be used for that electronics industry is hopeful and advantageous method.
Particularly, for example, common solid state growth method requires annealing steps at least 24 hours.Consider preferably 2 minutes each substrate processing time, pratical and feasible for making processing procedure, must want 15 annealing furnaces.The present invention can make process finish in 8 hours, and under optimum condition process even only can shorten to 4 hours or still less.As long as this stove number that has shown that process can be calculated in the above reduces to 6 or still less finish under the condition.This improves productivity ratio, cuts down equipment investment, thereby reduces the substrate producing cost.So, can produce economic TFT, this also permits and is referred to as new demand.As a result, the present invention is very useful to industry.
Very clear when the present invention consults special embodiment and is described in detail, to one skilled in the art to can make various changes and modification and can not depart from its spirit and scope.

Claims (29)

1. method of making semiconductor device, it comprises the steps:
A kind of catalyst material is partly contacted with a kind of selectivity that contains the semiconductor film of amorphous silicon, and described catalyst can promote this semiconductor film crystallization;
The described semiconductor film that has had catalyst material is annealed, so that this semiconductor film crystallization; And,
Top surface by described semiconductor film corrodes described catalyst material, makes this semiconductor film not be subjected to the effect of corrosion step basically.
2. method according to claim 1, wherein, described annealing is undertaken by heat treatment.
3. method according to claim 1 wherein, is removed excessive described catalyst material by described corrosion.
4. method according to claim 1, wherein, with 1 * 10 15Atom/centimetre 3To the concentration range of 1 atom %, described catalyst material is added in this semiconductor film, this concentration is measured with ion microprobe.
5. method according to claim 1, wherein, described catalyst material comprises a kind of metal, and this metal is selected from Pt, Fe, Co and Pd.
6. method according to claim 1 wherein, provides described catalyst material, and it is contacted with the following laminar surface of described semiconductor film.
7. method according to claim 1 wherein, provides described catalyst material, and it is contacted with the top surface of described semiconductor film.
8. method of making semiconductor device, it comprises the steps:
A kind of catalyst material is divided with a kind of selection portion that contains the semiconductor film of amorphous silicon contact, this catalyst can promote the crystallization of this semiconductor film;
The above-mentioned semiconductor film that has had described catalyst material is heated, so that this membrane crystallization; And,
With the described semiconductor film of laser radiation, increasing the degree of crystallinity of this semiconductor film,
Wherein, described method comprises that also top surface from described semiconductor film to the step that described catalyst material corrodes, makes described semiconductor film not be subjected to the effect of this corrosion step basically.
9. method according to claim 8 wherein, by described corrosion, is removed excessive described catalyst material.
10. method according to claim 8, wherein, with 1 * 10 15Atom/centimetre 3To the concentration range of 1 atom %, described catalyst material is added in the described semiconductor film, this concentration is measured with ion microprobe.
11. method according to claim 8, wherein, described catalyst material comprises a kind of metal, and this metal is selected from Pt, Fe, Co and Pd.
12. method according to claim 8 wherein, provides described catalyst material, and it is contacted with the following laminar surface of described semiconductor film.
13. method according to claim 8 wherein, provides described catalyst material, and it is contacted with the top surface of described semiconductor film.
14. a method of making semiconductor device, it comprises the steps:
A kind of catalyst material is divided with a kind of selection portion that contains the semiconductor film of amorphous silicon contact, this catalyst can promote the crystallization of this semiconductor film;
The semiconductor film that has described catalyst material is heated, so that this membrane crystallization; And
Described semiconductor film is carried out thermal annealing fast, so that further increase the degree of crystallinity of this semiconductor film;
Wherein, described method comprises that also top surface by semiconductor film to the step that catalyst material corrodes, makes described semiconductor film not be subjected to the effect of this corrosion step basically.
15. method according to claim 14 wherein, is removed excessive catalyst material by described corrosion.
16. method according to claim 14, wherein, with 1 * 10 15Atom/centimetre 3To the concentration range of 1 atom %, described semiconductor substance is added in the semiconductor film, this concentration is measured with ion microprobe.
17. method according to claim 14, wherein, described catalyst material comprises a kind of metal, and this metal is selected from Pt, Fe, Co and Pd.
18. method according to claim 14 wherein, provides described catalyst material, and it is contacted with the following laminar surface of semiconductor film.
19. method according to claim 14 wherein, provides described catalyst material, and it is contacted with the top surface of semiconductor film.
20. according to any one described method in the claim 1,8 or 14, wherein, described silicon fiml is an amorphous state.
21. want 1 or 7 method according to right, wherein, described silicon fiml comprises the channel region at least in the insulated-gate field-effect transistor, and, described material is formed at least on this channel region.
22. method according to claim 15, wherein, described silicon fiml comprises the channel region at least in the insulated-gate field-effect transistor, and, with described solvent coating on this channel region at least.
23. according to claim 1,8 or 14 described methods, wherein, the selection portion branch in the described semiconductor silicon fiml comprises the channel region at least of insulated-gate field-effect transistor, and, described catalyst is configured in the described at least selection district.
24. a method of making semiconductor device, it comprises the steps:
Dispose a kind of metallic catalyst, it is contacted with the surface of siliceous semiconductor film, this catalyst can promote the crystallization of semiconductor film;
The semiconductor film that has described catalyst material is heated, so that this membrane crystallization; And,
Then, after above-mentioned heating,, make this semiconductor film further carry out crystallization whereby with the described semiconductor film of laser radiation.
25. method according to claim 24 wherein, is disposed at a kind of selection district in the described semiconductor film with described catalyst, and, make crystalline growth by described heating, this crystallization with along with the surperficial parallel direction of this semiconductor film, by selecting the adjacent part growth in district with this.
26. method according to claim 24, wherein, described metal is selected from Ni, Fe, Co, Pt and Pd.
27. a method of making semiconductor device, it comprises the steps:
Dispose a kind of metallic catalyst, it is contacted with the surface of siliceous semiconductor film, described catalyst can promote the crystallization of this semiconductor film;
The semiconductor film that has above-mentioned catalyst material is heated, so that this membrane crystallization; And,
Then, after above-mentioned heating, carry out rapid thermal annealing, make the further crystallization of this semiconductor film whereby.
28. method according to claim 27, wherein, described catalyst is disposed at a kind of selection part in the described semiconductor film, and, make crystal growth by described heating, this crystal is by the described surface that is parallel to this semiconductor film, and grow by the position adjacent with this selection part.
29. method according to claim 27, wherein, described metal is selected from Ni, Fe, Co, Pt and Pd.
CNB001009435A 1993-02-15 2000-01-05 Manufacturing method of semiconductor device Expired - Lifetime CN1150595C (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP04853293A JP3562588B2 (en) 1993-02-15 1993-02-15 Method for manufacturing semiconductor device
JP48532/1993 1993-02-15

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
CN94103243A Division CN1058583C (en) 1993-02-15 1994-02-15 Semiconductor and process for fabricating the same

Publications (2)

Publication Number Publication Date
CN1291785A true CN1291785A (en) 2001-04-18
CN1150595C CN1150595C (en) 2004-05-19

Family

ID=12805981

Family Applications (4)

Application Number Title Priority Date Filing Date
CN94103243A Expired - Lifetime CN1058583C (en) 1993-02-15 1994-02-15 Semiconductor and process for fabricating the same
CNB001009443A Expired - Lifetime CN1156917C (en) 1993-02-15 1994-02-15 Semiconductor device and manufacture method
CNA2004100434859A Pending CN1540721A (en) 1993-02-15 1994-02-15 Semiconductor and process for fabricating same
CNB001009435A Expired - Lifetime CN1150595C (en) 1993-02-15 2000-01-05 Manufacturing method of semiconductor device

Family Applications Before (3)

Application Number Title Priority Date Filing Date
CN94103243A Expired - Lifetime CN1058583C (en) 1993-02-15 1994-02-15 Semiconductor and process for fabricating the same
CNB001009443A Expired - Lifetime CN1156917C (en) 1993-02-15 1994-02-15 Semiconductor device and manufacture method
CNA2004100434859A Pending CN1540721A (en) 1993-02-15 1994-02-15 Semiconductor and process for fabricating same

Country Status (4)

Country Link
US (3) US5879977A (en)
JP (1) JP3562588B2 (en)
KR (1) KR0169508B1 (en)
CN (4) CN1058583C (en)

Families Citing this family (116)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3562588B2 (en) 1993-02-15 2004-09-08 株式会社半導体エネルギー研究所 Method for manufacturing semiconductor device
JP3402380B2 (en) * 1993-03-22 2003-05-06 株式会社半導体エネルギー研究所 Semiconductor circuit and manufacturing method thereof
JP3329512B2 (en) * 1993-03-22 2002-09-30 株式会社半導体エネルギー研究所 Semiconductor circuit and manufacturing method thereof
JP3347804B2 (en) * 1993-03-22 2002-11-20 株式会社半導体エネルギー研究所 Method for manufacturing semiconductor circuit
US6713330B1 (en) 1993-06-22 2004-03-30 Semiconductor Energy Laboratory Co., Ltd. Method of fabricating a thin film transistor
US5488000A (en) 1993-06-22 1996-01-30 Semiconductor Energy Laboratory Co., Ltd. Method of fabricating a thin film transistor using a nickel silicide layer to promote crystallization of the amorphous silicon layer
US6074901A (en) * 1993-12-03 2000-06-13 Semiconductor Energy Laboratory Co., Ltd. Process for crystallizing an amorphous silicon film and apparatus for fabricating the same
KR100319332B1 (en) * 1993-12-22 2002-04-22 야마자끼 순페이 Semiconductor device and electro-optical device
JP3192546B2 (en) * 1994-04-15 2001-07-30 シャープ株式会社 Semiconductor device and method of manufacturing the same
JP3067949B2 (en) * 1994-06-15 2000-07-24 シャープ株式会社 Electronic device and liquid crystal display device
TW280943B (en) * 1994-07-15 1996-07-11 Sharp Kk
JP3072005B2 (en) * 1994-08-25 2000-07-31 シャープ株式会社 Semiconductor device and manufacturing method thereof
US6670640B1 (en) * 1994-09-15 2003-12-30 Semiconductor Energy Laboratory Co., Ltd. Method for producing semiconductor device
US5942768A (en) * 1994-10-07 1999-08-24 Semionductor Energy Laboratory Co., Ltd. Semiconductor device having improved crystal orientation
JP3277082B2 (en) * 1994-11-22 2002-04-22 シャープ株式会社 Semiconductor device and manufacturing method thereof
JP2900229B2 (en) * 1994-12-27 1999-06-02 株式会社半導体エネルギー研究所 Semiconductor device, manufacturing method thereof, and electro-optical device
US6331475B1 (en) 1995-01-12 2001-12-18 Semiconductor Energy Laboratory Co., Ltd. Method and manufacturing semiconductor device
JPH0927452A (en) * 1995-07-12 1997-01-28 Semiconductor Energy Lab Co Ltd Manufacture of semiconductor device
US5854803A (en) * 1995-01-12 1998-12-29 Semiconductor Energy Laboratory Co., Ltd. Laser illumination system
TW344901B (en) * 1995-02-15 1998-11-11 Handotai Energy Kenkyusho Kk Active matrix display device
US6011607A (en) * 1995-02-15 2000-01-04 Semiconductor Energy Laboratory Co., Active matrix display with sealing material
TW345654B (en) 1995-02-15 1998-11-21 Handotai Energy Kenkyusho Kk Active matrix display device
US5757456A (en) 1995-03-10 1998-05-26 Semiconductor Energy Laboratory Co., Ltd. Display device and method of fabricating involving peeling circuits from one substrate and mounting on other
JP3138169B2 (en) * 1995-03-13 2001-02-26 シャープ株式会社 Method for manufacturing semiconductor device
US5834327A (en) 1995-03-18 1998-11-10 Semiconductor Energy Laboratory Co., Ltd. Method for producing display device
KR100265179B1 (en) 1995-03-27 2000-09-15 야마자끼 순페이 Semiconductor device and manufacturing method thereof
TW297138B (en) * 1995-05-31 1997-02-01 Handotai Energy Kenkyusho Kk
TW529773U (en) 1995-06-01 2003-04-21 Semiconductor Energy L B Semiconductor device
US6902616B1 (en) 1995-07-19 2005-06-07 Semiconductor Energy Laboratory Co., Ltd. Method and apparatus for producing semiconductor device
US6228751B1 (en) 1995-09-08 2001-05-08 Semiconductor Energy Laboratory Co., Ltd. Method of manufacturing a semiconductor device
JP3174486B2 (en) * 1995-09-08 2001-06-11 シャープ株式会社 Solar cell and method of manufacturing the same
TW371796B (en) 1995-09-08 1999-10-11 Semiconductor Energy Lab Co Ltd Method and apparatus for manufacturing a semiconductor device
JPH09146108A (en) * 1995-11-17 1997-06-06 Semiconductor Energy Lab Co Ltd Liquid crystal display device and its driving method
JPH09171192A (en) 1995-12-19 1997-06-30 Semiconductor Energy Lab Co Ltd Active matrix type liquid crystal display device and its manufacture
JP3477301B2 (en) 1995-12-19 2003-12-10 株式会社半導体エネルギー研究所 Active matrix type liquid crystal display device and manufacturing method thereof
JP3645380B2 (en) * 1996-01-19 2005-05-11 株式会社半導体エネルギー研究所 Manufacturing method of semiconductor device, information terminal, head mounted display, navigation system, mobile phone, video camera, projection display device
JP3729955B2 (en) * 1996-01-19 2005-12-21 株式会社半導体エネルギー研究所 Method for manufacturing semiconductor device
JP3645379B2 (en) * 1996-01-19 2005-05-11 株式会社半導体エネルギー研究所 Method for manufacturing semiconductor device
US7056381B1 (en) * 1996-01-26 2006-06-06 Semiconductor Energy Laboratory Co., Ltd. Fabrication method of semiconductor device
US6449024B1 (en) 1996-01-26 2002-09-10 Semiconductor Energy Laboratory Co., Inc. Liquid crystal electro-optical device utilizing a polymer with an anisotropic refractive index
JP3301054B2 (en) * 1996-02-13 2002-07-15 株式会社半導体エネルギー研究所 Laser irradiation device and laser irradiation method
JP3698809B2 (en) 1996-03-23 2005-09-21 株式会社半導体エネルギー研究所 Liquid crystal device manufacturing method
JPH10228248A (en) 1996-12-09 1998-08-25 Semiconductor Energy Lab Co Ltd Active matrix display device and its manufacture
JP3917698B2 (en) 1996-12-12 2007-05-23 株式会社半導体エネルギー研究所 Laser annealing method and laser annealing apparatus
JPH10199807A (en) 1996-12-27 1998-07-31 Semiconductor Energy Lab Co Ltd Manufacture of crystalline silicon film
US6140166A (en) * 1996-12-27 2000-10-31 Semicondutor Energy Laboratory Co., Ltd. Method for manufacturing semiconductor and method for manufacturing semiconductor device
JPH10198292A (en) 1996-12-30 1998-07-31 Semiconductor Energy Lab Co Ltd Semiconductor device and its manufacture
JP3976828B2 (en) 1997-02-17 2007-09-19 株式会社半導体エネルギー研究所 Method for producing crystalline silicon film
JP3844552B2 (en) * 1997-02-26 2006-11-15 株式会社半導体エネルギー研究所 Method for manufacturing semiconductor device
JP3544280B2 (en) 1997-03-27 2004-07-21 株式会社半導体エネルギー研究所 Method for manufacturing semiconductor device
JP4059952B2 (en) * 1997-03-27 2008-03-12 株式会社半導体エネルギー研究所 Laser light irradiation method
JP4086932B2 (en) 1997-04-17 2008-05-14 株式会社半導体エネルギー研究所 Laser irradiation apparatus and laser processing method
JP3770999B2 (en) * 1997-04-21 2006-04-26 株式会社半導体エネルギー研究所 Laser irradiation apparatus and laser irradiation method
AUPO638997A0 (en) * 1997-04-23 1997-05-22 Unisearch Limited Metal contact scheme using selective silicon growth
US6465268B2 (en) 1997-05-22 2002-10-15 Semiconductor Energy Laboratory Co., Ltd. Method of manufacturing an electro-optical device
US6307214B1 (en) 1997-06-06 2001-10-23 Semiconductor Energy Laboratory Co., Ltd. Semiconductor thin film and semiconductor device
US6501094B1 (en) * 1997-06-11 2002-12-31 Semiconductor Energy Laboratory Co., Ltd. Semiconductor device comprising a bottom gate type thin film transistor
US6066547A (en) * 1997-06-20 2000-05-23 Sharp Laboratories Of America, Inc. Thin-film transistor polycrystalline film formation by nickel induced, rapid thermal annealing method
US6316357B1 (en) * 1997-10-08 2001-11-13 Industrial Technology Research Institute Method for forming metal silicide by laser irradiation
US6060392A (en) * 1998-02-11 2000-05-09 National Semiconductor Corporation Fabrication of silicides by excimer laser annealing of amorphous silicon
US6246524B1 (en) 1998-07-13 2001-06-12 Semiconductor Energy Laboratory Co., Ltd. Beam homogenizer, laser irradiation apparatus, laser irradiation method, and method of manufacturing semiconductor device
JP4663047B2 (en) 1998-07-13 2011-03-30 株式会社半導体エネルギー研究所 Laser irradiation apparatus and method for manufacturing semiconductor device
US7153729B1 (en) * 1998-07-15 2006-12-26 Semiconductor Energy Laboratory Co., Ltd. Crystalline semiconductor thin film, method of fabricating the same, semiconductor device, and method of fabricating the same
US7294535B1 (en) * 1998-07-15 2007-11-13 Semiconductor Energy Laboratory Co., Ltd. Crystalline semiconductor thin film, method of fabricating the same, semiconductor device, and method of fabricating the same
US7084016B1 (en) * 1998-07-17 2006-08-01 Semiconductor Energy Laboratory Co., Ltd. Crystalline semiconductor thin film, method of fabricating the same, semiconductor device, and method of fabricating the same
US7282398B2 (en) * 1998-07-17 2007-10-16 Semiconductor Energy Laboratory Co., Ltd. Crystalline semiconductor thin film, method of fabricating the same, semiconductor device and method of fabricating the same
JP2000058839A (en) 1998-08-05 2000-02-25 Semiconductor Energy Lab Co Ltd Semiconductor device provided with semiconductor circuit composed of semiconductor element and its manufacture
US6559036B1 (en) 1998-08-07 2003-05-06 Semiconductor Energy Laboratory Co., Ltd. Semiconductor device and method of manufacturing the same
US6294441B1 (en) 1998-08-18 2001-09-25 Semiconductor Energy Laboratory Co., Ltd. Method of manufacturing a semiconductor device
JP2000174282A (en) * 1998-12-03 2000-06-23 Semiconductor Energy Lab Co Ltd Semiconductor device
US6380007B1 (en) 1998-12-28 2002-04-30 Semiconductor Energy Laboratory Co., Ltd. Semiconductor device and manufacturing method of the same
US6393042B1 (en) 1999-03-08 2002-05-21 Semiconductor Energy Laboratory Co., Ltd. Beam homogenizer and laser irradiation apparatus
US6878968B1 (en) 1999-05-10 2005-04-12 Semiconductor Energy Laboratory Co., Ltd. Semiconductor device
JP4298131B2 (en) * 1999-05-14 2009-07-15 株式会社半導体エネルギー研究所 Method for manufacturing liquid crystal display device
US6680487B1 (en) 1999-05-14 2004-01-20 Semiconductor Energy Laboratory Co., Ltd. Semiconductor comprising a TFT provided on a substrate having an insulating surface and method of fabricating the same
JP4666723B2 (en) 1999-07-06 2011-04-06 株式会社半導体エネルギー研究所 Method for manufacturing semiconductor device
TW459275B (en) * 1999-07-06 2001-10-11 Semiconductor Energy Lab Semiconductor device and method of fabricating the same
US6440851B1 (en) * 1999-10-12 2002-08-27 International Business Machines Corporation Method and structure for controlling the interface roughness of cobalt disilicide
US7232742B1 (en) 1999-11-26 2007-06-19 Semiconductor Energy Laboratory Co., Ltd. Method of manufacturing a semiconductor device that includes forming a material with a high tensile stress in contact with a semiconductor film to getter impurities from the semiconductor film
US6844910B2 (en) 1999-12-28 2005-01-18 Semiconductor Energy Laboratory Co., Ltd. Liquid crystal display device and manufacturing method thereof
KR100660814B1 (en) * 1999-12-31 2006-12-26 엘지.필립스 엘시디 주식회사 method for fabricating semiconductor layer for thin film transistor
US7071041B2 (en) * 2000-01-20 2006-07-04 Semiconductor Energy Laboratory Co., Ltd. Method of manufacturing a semiconductor device
KR100450595B1 (en) 2000-02-09 2004-09-30 히다찌 케이블 리미티드 Crystalline silicon semiconductor device and method for fabricating same
US7098084B2 (en) * 2000-03-08 2006-08-29 Semiconductor Energy Laboratory Co., Ltd. Semiconductor device and manufacturing method thereof
US6916693B2 (en) * 2000-03-08 2005-07-12 Semiconductor Energy Laboratory Co., Ltd. Semiconductor device and manufacturing method thereof
GB0006958D0 (en) * 2000-03-23 2000-05-10 Koninkl Philips Electronics Nv Method of manufacturing a transistor
US6770518B2 (en) * 2001-01-29 2004-08-03 Semiconductor Energy Laboratory Co., Ltd. Method for manufacturing a semiconductor device
SG114529A1 (en) * 2001-02-23 2005-09-28 Semiconductor Energy Lab Method of manufacturing a semiconductor device
SG143975A1 (en) * 2001-02-28 2008-07-29 Semiconductor Energy Lab Method of manufacturing a semiconductor device
US6830994B2 (en) * 2001-03-09 2004-12-14 Semiconductor Energy Laboratory Co., Ltd. Method of manufacturing a semiconductor device having a crystallized semiconductor film
JP2003282438A (en) * 2002-03-27 2003-10-03 Seiko Epson Corp Semiconductor device and manufacturing method thereof, electro-optical device, and electronic equipment
US7335255B2 (en) * 2002-11-26 2008-02-26 Semiconductor Energy Laboratory, Co., Ltd. Manufacturing method of semiconductor device
KR100534579B1 (en) * 2003-03-05 2005-12-07 삼성에스디아이 주식회사 Polysilicon thin film, method of fabricating the same and thin film transistor non-dependancy on active channel direction
US7348222B2 (en) * 2003-06-30 2008-03-25 Semiconductor Energy Laboratory Co., Ltd. Method for manufacturing a thin film transistor and method for manufacturing a semiconductor device
US7247527B2 (en) * 2003-07-31 2007-07-24 Semiconductor Energy Laboratory Co., Ltd. Method for manufacturing semiconductor device, and laser irradiation apparatus
US7358165B2 (en) * 2003-07-31 2008-04-15 Semiconductor Energy Laboratory Co., Ltd Semiconductor device and method for manufacturing semiconductor device
CN100423199C (en) * 2003-10-16 2008-10-01 Jsr株式会社 Composition for forming silicon-cobalt film, silicon-cobalt film, and forming method therefor
US7964925B2 (en) * 2006-10-13 2011-06-21 Hewlett-Packard Development Company, L.P. Photodiode module and apparatus including multiple photodiode modules
JP4094539B2 (en) * 2003-12-12 2008-06-04 株式会社半導体エネルギー研究所 Method for manufacturing semiconductor integrated circuit
JP4339102B2 (en) * 2003-12-12 2009-10-07 株式会社半導体エネルギー研究所 Method for manufacturing display device
US7276402B2 (en) * 2003-12-25 2007-10-02 Semiconductor Energy Laboratory Co., Ltd. Semiconductor device and manufacturing method thereof
US7507617B2 (en) * 2003-12-25 2009-03-24 Semiconductor Energy Laboratory Co., Ltd. Method for manufacturing semiconductor device
CN1691277B (en) * 2004-03-26 2010-05-26 株式会社半导体能源研究所 Method for manufacturing semiconductor device
CN100359651C (en) * 2004-05-17 2008-01-02 统宝光电股份有限公司 Polycrystalline silicon annealing arrangement applied to high-performance thin film transistor and method thereof
KR100712101B1 (en) * 2004-06-30 2007-05-02 삼성에스디아이 주식회사 Thin Film Transistor and Method of fabricating thereof
US7291522B2 (en) * 2004-10-28 2007-11-06 Hewlett-Packard Development Company, L.P. Semiconductor devices and methods of making
US7381600B2 (en) * 2004-12-02 2008-06-03 The Hong Kong University Of Science And Technology Method of annealing polycrystalline silicon using solid-state laser and devices built thereon
JP4734944B2 (en) * 2005-02-02 2011-07-27 セイコーエプソン株式会社 Method for manufacturing thin film semiconductor device
US8088676B2 (en) * 2005-04-28 2012-01-03 The Hong Kong University Of Science And Technology Metal-induced crystallization of amorphous silicon, polycrystalline silicon thin films produced thereby and thin film transistors produced therefrom
US20070117287A1 (en) * 2005-11-23 2007-05-24 Semiconductor Energy Laboratory Co., Ltd. Laser irradiation apparatus
US20080095975A1 (en) * 2006-10-23 2008-04-24 Jin Jang Polycrystalline silicon thin film and method for forming the same
JP4799509B2 (en) * 2007-08-16 2011-10-26 株式会社半導体エネルギー研究所 Peeling method
JP2010182841A (en) * 2009-02-05 2010-08-19 Sony Corp Method of forming semiconductor thin film and inspection device for semiconductor thin film
WO2014141662A1 (en) 2013-03-13 2014-09-18 Okinawa Institute Of Science And Technology School Corporation Metal induced nanocrystallization of amorphous semiconductor quantum dots
KR102098588B1 (en) * 2013-06-28 2020-04-08 삼성전자주식회사 Semiconductor Device and Method for manufacturing the same
US9275866B2 (en) 2014-05-15 2016-03-01 International Business Machines Corporation Gas cluster reactor for anisotropic film growth

Family Cites Families (71)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2316095A1 (en) * 1973-03-30 1974-10-10 Siemens Ag METHOD FOR MANUFACTURING INTEGRATED CIRCUITS WITH COMPLEMENTARY CHANNEL FIELD EFFECT TRANSISTORS
CH579827A5 (en) * 1974-11-04 1976-09-15 Bbc Brown Boveri & Cie
US4215156A (en) * 1977-08-26 1980-07-29 International Business Machines Corporation Method for fabricating tantalum semiconductor contacts
US4231809A (en) * 1979-05-25 1980-11-04 Bell Telephone Laboratories, Incorporated Method of removing impurity metals from semiconductor devices
US4331485A (en) * 1980-03-03 1982-05-25 Arnon Gat Method for heat treating semiconductor material using high intensity CW lamps
US4379020A (en) * 1980-06-16 1983-04-05 Massachusetts Institute Of Technology Polycrystalline semiconductor processing
JPS5734331A (en) * 1980-08-11 1982-02-24 Toshiba Corp Manufacture of semiconductor device
DE3272410D1 (en) 1981-02-16 1986-09-11 Fujitsu Ltd Method of producing mosfet type semiconductor device
AT380974B (en) * 1982-04-06 1986-08-11 Shell Austria METHOD FOR SETTING SEMICONDUCTOR COMPONENTS
US4481121A (en) * 1982-05-17 1984-11-06 Hughes Tool Company Viscosifier for oil base drilling fluids
EP0197531B1 (en) * 1985-04-08 1993-07-28 Hitachi, Ltd. Thin film transistor formed on insulating substrate
JPS63142807A (en) * 1986-12-05 1988-06-15 Nec Corp Manufacture of semiconductor device
US5169680A (en) * 1987-05-07 1992-12-08 Intel Corporation Electroless deposition for IC fabrication
US4758533A (en) * 1987-09-22 1988-07-19 Xmr Inc. Laser planarization of nonrefractory metal during integrated circuit fabrication
JPH01187875A (en) * 1988-01-22 1989-07-27 Seiko Epson Corp Manufacture of semiconductor device
JP2638869B2 (en) * 1988-01-22 1997-08-06 セイコーエプソン株式会社 Method for manufacturing semiconductor device
US5407867A (en) * 1988-05-12 1995-04-18 Mitsubishki Denki Kabushiki Kaisha Method of forming a thin film on surface of semiconductor substrate
JPH02140915A (en) * 1988-11-22 1990-05-30 Seiko Epson Corp Manufacture of semiconductor device
JPH02260521A (en) 1989-03-31 1990-10-23 Canon Inc Article having polycrystalline si semiconductor thin film and manufacture thereof
DE69033153T2 (en) 1989-03-31 1999-11-11 Canon Kk Method for producing a semiconductor thin film and semiconductor thin film produced therewith
JPH02275641A (en) * 1989-04-17 1990-11-09 Seiko Epson Corp Manufacture of semiconductor device
US5278093A (en) * 1989-09-23 1994-01-11 Canon Kabushiki Kaisha Method for forming semiconductor thin film
JPH03280418A (en) * 1990-03-28 1991-12-11 Seiko Epson Corp Manufacture of semiconductor film
JPH0760807B2 (en) * 1990-03-29 1995-06-28 株式会社ジーティシー Method for manufacturing semiconductor thin film
JP2575545B2 (en) * 1990-07-05 1997-01-29 株式会社東芝 Method for manufacturing semiconductor device
US5147826A (en) * 1990-08-06 1992-09-15 The Pennsylvania Research Corporation Low temperature crystallization and pattering of amorphous silicon films
JP3333187B2 (en) 1990-08-18 2002-10-07 セイコーエプソン株式会社 Method for manufacturing thin film semiconductor device
US5112764A (en) * 1990-09-04 1992-05-12 North American Philips Corporation Method for the fabrication of low leakage polysilicon thin film transistors
US5560804A (en) * 1991-03-19 1996-10-01 Tokyo Electron Limited Etching method for silicon containing layer
JPH04348035A (en) * 1991-05-24 1992-12-03 Nippon Steel Corp Wiring forming method
JPH0567635A (en) 1991-09-09 1993-03-19 Oki Electric Ind Co Ltd Manufacture of semiconductor device
US5244819A (en) * 1991-10-22 1993-09-14 Honeywell Inc. Method to getter contamination in semiconductor devices
JP3280418B2 (en) 1992-06-25 2002-05-13 松下電工株式会社 Hair cutter
JP3280420B2 (en) 1992-07-30 2002-05-13 株式会社紀文フードケミファ Calcium absorption promoting composition containing soy milk
US5272119A (en) * 1992-09-23 1993-12-21 Memc Electronic Materials, Spa Process for contamination removal and minority carrier lifetime improvement in silicon
US5604360A (en) * 1992-12-04 1997-02-18 Semiconductor Energy Laboratory Co., Ltd. Semiconductor device including a plurality of thin film transistors at least some of which have a crystalline silicon film crystal-grown substantially in parallel to the surface of a substrate for the transistor
TW226478B (en) * 1992-12-04 1994-07-11 Semiconductor Energy Res Co Ltd Semiconductor device and method for manufacturing the same
JPH06296023A (en) * 1993-02-10 1994-10-21 Semiconductor Energy Lab Co Ltd Thin-film semiconductor device and manufacture thereof
US5639698A (en) * 1993-02-15 1997-06-17 Semiconductor Energy Laboratory Co., Ltd. Semiconductor, semiconductor device, and method for fabricating the same
JP3562588B2 (en) * 1993-02-15 2004-09-08 株式会社半導体エネルギー研究所 Method for manufacturing semiconductor device
US5275851A (en) * 1993-03-03 1994-01-04 The Penn State Research Foundation Low temperature crystallization and patterning of amorphous silicon films on electrically insulating substrates
CN1095204C (en) * 1993-03-12 2002-11-27 株式会社半导体能源研究所 Transistor and process for fabricating the same
US5569936A (en) * 1993-03-12 1996-10-29 Semiconductor Energy Laboratory Co., Ltd. Semiconductor device employing crystallization catalyst
TW241377B (en) * 1993-03-12 1995-02-21 Semiconductor Energy Res Co Ltd
US5624851A (en) * 1993-03-12 1997-04-29 Semiconductor Energy Laboratory Co., Ltd. Process of fabricating a semiconductor device in which one portion of an amorphous silicon film is thermally crystallized and another portion is laser crystallized
JP3193803B2 (en) * 1993-03-12 2001-07-30 株式会社半導体エネルギー研究所 Manufacturing method of semiconductor element
US5501989A (en) * 1993-03-22 1996-03-26 Semiconductor Energy Laboratory Co., Ltd. Method of making semiconductor device/circuit having at least partially crystallized semiconductor layer
US5481121A (en) * 1993-05-26 1996-01-02 Semiconductor Energy Laboratory Co., Ltd. Semiconductor device having improved crystal orientation
US5488000A (en) * 1993-06-22 1996-01-30 Semiconductor Energy Laboratory Co., Ltd. Method of fabricating a thin film transistor using a nickel silicide layer to promote crystallization of the amorphous silicon layer
US5663077A (en) * 1993-07-27 1997-09-02 Semiconductor Energy Laboratory Co., Ltd. Method of manufacturing a thin film transistor in which the gate insulator comprises two oxide films
US5529937A (en) * 1993-07-27 1996-06-25 Semiconductor Energy Laboratory Co., Ltd. Process for fabricating thin film transistor
US5492843A (en) * 1993-07-31 1996-02-20 Semiconductor Energy Laboratory Co., Ltd. Method of fabricating semiconductor device and method of processing substrate
JP2975973B2 (en) * 1993-08-10 1999-11-10 株式会社半導体エネルギー研究所 Semiconductor device and manufacturing method thereof
JP2762215B2 (en) * 1993-08-12 1998-06-04 株式会社半導体エネルギー研究所 Method for manufacturing thin film transistor and semiconductor device
JP2814049B2 (en) * 1993-08-27 1998-10-22 株式会社半導体エネルギー研究所 Semiconductor device and manufacturing method thereof
TW264575B (en) * 1993-10-29 1995-12-01 Handotai Energy Kenkyusho Kk
JP3562590B2 (en) * 1993-12-01 2004-09-08 株式会社半導体エネルギー研究所 Semiconductor device manufacturing method
US5612250A (en) * 1993-12-01 1997-03-18 Semiconductor Energy Laboratory Co., Ltd. Method for manufacturing a semiconductor device using a catalyst
US5654203A (en) * 1993-12-02 1997-08-05 Semiconductor Energy Laboratory, Co., Ltd. Method for manufacturing a thin film transistor using catalyst elements to promote crystallization
JP2860869B2 (en) * 1993-12-02 1999-02-24 株式会社半導体エネルギー研究所 Semiconductor device and manufacturing method thereof
KR100319332B1 (en) * 1993-12-22 2002-04-22 야마자끼 순페이 Semiconductor device and electro-optical device
TW279275B (en) * 1993-12-27 1996-06-21 Sharp Kk
JP3378078B2 (en) * 1994-02-23 2003-02-17 株式会社半導体エネルギー研究所 Method for manufacturing semiconductor device
JPH07335906A (en) * 1994-06-14 1995-12-22 Semiconductor Energy Lab Co Ltd Thin film semiconductor device and fabrication thereof
JP3072000B2 (en) * 1994-06-23 2000-07-31 株式会社半導体エネルギー研究所 Method for manufacturing semiconductor device
JP3897826B2 (en) * 1994-08-19 2007-03-28 株式会社半導体エネルギー研究所 Active matrix display device
US5712191A (en) * 1994-09-16 1998-01-27 Semiconductor Energy Laboratory Co., Ltd. Method for producing semiconductor device
JP3942651B2 (en) * 1994-10-07 2007-07-11 株式会社半導体エネルギー研究所 Method for manufacturing semiconductor device
JP3486240B2 (en) * 1994-10-20 2004-01-13 株式会社半導体エネルギー研究所 Semiconductor device
US5756364A (en) * 1994-11-29 1998-05-26 Semiconductor Energy Laboratory Co., Ltd. Laser processing method of semiconductor device using a catalyst
TW447144B (en) * 1995-03-27 2001-07-21 Semiconductor Energy Lab Semiconductor device and a method of manufacturing the same

Also Published As

Publication number Publication date
CN1540721A (en) 2004-10-27
CN1150595C (en) 2004-05-19
CN1058583C (en) 2000-11-15
US6110770A (en) 2000-08-29
US5879977A (en) 1999-03-09
KR0169508B1 (en) 1999-02-01
CN1264180A (en) 2000-08-23
CN1098556A (en) 1995-02-08
CN1156917C (en) 2004-07-07
JPH06244104A (en) 1994-09-02
US6451638B1 (en) 2002-09-17
JP3562588B2 (en) 2004-09-08

Similar Documents

Publication Publication Date Title
CN1058583C (en) Semiconductor and process for fabricating the same
US7435635B2 (en) Method for crystallizing semiconductor material
US5962869A (en) Semiconductor material and method for forming the same and thin film transistor
US5147826A (en) Low temperature crystallization and pattering of amorphous silicon films
JP2006066860A (en) Manufacturing method for thin film transistor
US20010051416A1 (en) Semiconductor material and method for forming the same and thin film transistor
JP3300153B2 (en) Method for manufacturing semiconductor device
KR100994236B1 (en) Manufacturing method for thin film of poly-crystalline silicon
KR100611761B1 (en) Method fabricating thin film transistor
CN1727525A (en) A kind of method for preparing polysilicon
KR19980036973A (en) Method of manufacturing polycrystalline thin film using microwave
JP2009135488A (en) Crystallization method of silicon
KR101919086B1 (en) Method for forming polycrystalline silicon films
KR20130060002A (en) Manufacturing method for thin film of poly-crystalline material
KR101064325B1 (en) Manufacturing method for thin film of poly-crystalline silicon
KR101011806B1 (en) Manufacturing method for thin film of poly-crystalline silicon
TWI451479B (en) Manufacturing method for thin film of poly-crystalline silicon
KR100425857B1 (en) Method of crystallizing amorphous silicon thin film using crystallization inducing thin film with minimum thickness and concentration
TWI377173B (en) Method for manufacturing crystalline silicon
US20080095975A1 (en) Polycrystalline silicon thin film and method for forming the same
KR101131216B1 (en) Manufacturing method for thin film of poly-crystalline silicon
KR101123373B1 (en) Manufacturing method for thin film of poly-crystalline silicon
KR101131217B1 (en) Manufacturing method for thin film of poly-crystalline silicon
KR101117291B1 (en) Manufacturing method for thin film of poly-crystalline silicon
KR101090144B1 (en) Poly silicon film and methods of manufacturing the same

Legal Events

Date Code Title Description
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C06 Publication
PB01 Publication
C14 Grant of patent or utility model
GR01 Patent grant
CX01 Expiry of patent term

Expiration termination date: 20140215

Granted publication date: 20040519

CX01 Expiry of patent term